Optimal systemic therapy in men with low-volume prostate cancer

被引:1
作者
Saxena, Akshat [1 ]
Andrews, Jack [2 ]
Bryce, Alan Haruo [3 ]
Riaz, Irbaz Bin [1 ]
机构
[1] Mayo Clin, Dept Oncol, Scottsdale, AZ USA
[2] Mayo Clin, Dept Urol, Scottsdale, AZ USA
[3] City Hope Canc Ctr, Dept Oncol, Goodyear, AZ USA
关键词
hormone sensitive prostate cancer; low volume; metastatic prostate cancer; systemic therapy; STEREOTACTIC BODY RADIOTHERAPY; PHASE-II TRIAL; CELL-FREE DNA; ABIRATERONE ACETATE; MULTICENTER; METASTASES; ASSOCIATION; RECURRENCE; RESISTANCE; DIAGNOSIS;
D O I
10.1097/MOU.0000000000001165
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose of reviewLow-volume prostate cancer is an established prognostic category of metastatic hormone-sensitive prostate cancer. However, the term is often loosely used to reflect the low burden of disease across different prostate cancer states. This review explores the definitions of low-volume prostate cancer, biology, and current evidence for treatment. We also explore future directions, including the impact of advanced imaging modalities, particularly prostate-specific membrane antigen (PSMA) positron emission tomography (PET) scans, on refining patient subgroups and treatment strategies for patients with low-volume prostate cancer.Recent findingsRecent investigations have attempted to redefine low-volume disease, incorporating factors beyond metastatic burden. Advanced imaging, especially PSMA PET, offers enhanced accuracy in detecting metastases, potentially challenging the conventional definition of low volume. The prognosis and treatment of low-volume prostate cancer may vary by the timing of metastatic presentation. Biomarker-directed consolidative therapy, metastases-directed therapy, and de-escalation of systemic therapies will be increasingly important, especially in patients with metachronous low-volume disease.SummaryIn the absence of validated biomarkers, the management of low-volume prostate cancer as defined by CHAARTED criteria may be guided by the timing of metastatic presentation. For metachronous low-volume disease, we recommend novel hormonal therapy (NHT) doublets with or without consolidative metastasis-directed therapy (MDT), and for synchronous low-volume disease, NHT doublets with or without consolidative MDT and prostate-directed radiation. Docetaxel triplets may be a reasonable alternative in some patients with synchronous presentation. There is no clear role of docetaxel doublets in patients with low-volume disease. In the future, a small subset of low-volume diseases with oligometastases selected by genomics and advanced imaging like PSMA PET may achieve long-term remission with MDT with no systemic therapy.
引用
收藏
页码:183 / 197
页数:15
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